首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Atypical teratoid/rhabdoid tumors may show morphological and immunohistochemical features seen in choroid plexus tumors.
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Atypical teratoid/rhabdoid tumors may show morphological and immunohistochemical features seen in choroid plexus tumors.

机译:非典型的类畸形/类胡萝卜素肿瘤可能显示出脉络丛神经肿瘤的形态学和免疫组化特征。

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摘要

Atypical teratoid/rhabdoid tumors (AT/RT) are aggressive embryonal tumors having a poor prognosis and are associated with mutations in the tumor suppressor gene hSNF5/SMARCB1/INI1. Differential diagnosis includes choroid plexus carcinoma which has occasionally been attributed as showing an inactivation of INI1/SMARCB1 nuclear staining in immunohistochemistry. However, these findings have been challenged by others. We therefore examined eight AT/RTs from six patients by immunohistochemistry for membranous expression of the inward rectifier potassium channel Kir7.1, which was in the central nervous system so far considered specific for choroid plexus tumors and normal choroid plexus epithelium. Two AT/RT cases exhibited membranous staining of Kir7.1, indicating a plexus epithelial differentiation of these tumors. The implications of these results on tumor diagnosis are discussed.
机译:非典型的类畸形/类胡萝卜瘤(AT / RT)是预后较差的侵袭性胚胎肿瘤,与肿瘤抑制基因hSNF5 / SMARCB1 / INI1的突变有关。鉴别诊断包括脉络丛癌,该脉络丛癌有时被归因于在免疫组织化学中显示INI1 / SMARCB1核染色失活。但是,这些发现受到了其他方面的挑战。因此,我们通过免疫组织化学检查了来自六名患者的八个AT / RTs的内向整流钾通道Kir7.1的膜表达,该通道目前在中枢神经系统中被认为对脉络丛肿瘤和正常脉络丛上皮具有特异性。 2例AT / RT病例表现出Kir7.1的膜性染色,表明这些肿瘤的神经丛上皮分化。讨论了这些结果对肿瘤诊断的意义。

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